Clinical Trials Logo

Acute Severe Respiratory Failure clinical trials

View clinical trials related to Acute Severe Respiratory Failure.

Filter by:
  • None
  • Page 1

NCT ID: NCT03415529 Completed - Clinical trials for Acute Respiratory Distress Syndrome

Impact of Arterial CO2 Tension on Management and Outcome in Patients With Acute Hypoxemic Respirator Failure and ARDS

CO2 LUNG SAFE
Start date: March 1, 2018
Phase:
Study type: Observational

There appears to be considerable variability in the approach physicians use to manage arterial carbon dioxide tensions, in patients in the early phases [first 48 hours] of ARDS (Acute hypoxemic respiratory failure and). A number of specific concerns exist, particularly the use of greater than needed inspired oxygen concentrations (potentially in 40% patients), and the proportion of hypocapnic patients in our cohort.

NCT ID: NCT03255109 Completed - Clinical trials for Acute Respiratory Distress Syndrome

WorldwidE AssessmeNt of Separation of pAtients From Ventilatory assistancE

WEAN SAFE
Start date: October 1, 2017
Phase:
Study type: Observational [Patient Registry]

WEAN SAFE (WorldwidE AssessmeNt of Separation of pAtients From ventilatory assistancE) is a multi-centre, prospective, observational, 4-week inception cohort study being carried out by the Acute Respiratory Failure section of ESICM. Weaning represents a challenge for intensivists and patients spend a considerable amount of time in being liberated from mechanical ventilation. While guidelines do exist on the classification of weaning, a recent study has shown that these may not be applicable to all patients. Moreover, different practices exist in regard to weaning procedures. WEAN SAFE will prospectively assess the burden of, management and spectrum of approaches to weaning from ventilation, in patients that require invasive mechanical ventilation for any reason, for a time period of at least 24 hours.

NCT ID: NCT02010073 Completed - Clinical trials for Acute Respiratory Distress Syndrome

Large Observational Study to UNderstand the Global Impact of Severe Acute Respiratory FailurE

LUNG-SAFE
Start date: February 2014
Phase: N/A
Study type: Observational

We wish to prospectively assess the burden of, management and therapeutic approaches to, and outcomes from acute hypoxaemic respiratory failure requiring ventilatory support, during the winter months in both the northern and southern hemispheres. We wish to specifically examine the contribution of ARDS as defined by the Berlin Definition to the burden of hypoxaemic respiratory failure. Why? The purpose of this study is to provide new and current data on the disease burden of acute hypoxemic respiratory failure and ARDS. It will answer the following questions: - What is the frequency and disease burden of acute hypoxaemic respiratory failure in winter? - What are the aetiologies of acute hypoxaemic respiratory failure requiring ventilatory support? - What is the incidence of ARDS based on the Berlin definition within this patient cohort? - What is the mortality from ARDS within this cohort, and how does this vary based on ARDS severity? - What is the natural history of ARDS? - What are the key patterns of therapeutic resource utilization, particularly approaches to sustain gas exchange, in these patients? When? The study is performed over a 4 week period between February 1st and March 31st 2014 in the Northern Hemisphere and June 1st to August 31st in the Southern Hemisphere. What data is required? A basic dataset is collected on all patients admitted with acute acute hypoxaemic respiratory failure requiring ventilatory support, with a more detailed dataset collected on patients diagnosed with ARDS.